FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0007307> ?p ?o ?g. }

• MONDO_0007307 hasDbXref "DOID:0110152" @default.
• MONDO_0007307 hasDbXref "GARD:1246" @default.
• MONDO_0007307 hasDbXref "NCIT:C118782" @default.
• MONDO_0007307 hasDbXref "OMIM:118200" @default.
• MONDO_0007307 hasDbXref "Orphanet:101082" @default.
• MONDO_0007307 hasDbXref "UMLS:C0270912" @default.
• MONDO_0007307 hasExactSynonym "CMT1B" @default.
• MONDO_0007307 hasExactSynonym "Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy" @default.
• MONDO_0007307 hasExactSynonym "Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ" @default.
• MONDO_0007307 hasExactSynonym "Charcot-Marie-Tooth disease, type 1B" @default.
• MONDO_0007307 hasExactSynonym "Charcot-Marie-Tooth neuropathy type 1B" @default.
• MONDO_0007307 hasExactSynonym "HMSN IB" @default.
• MONDO_0007307 hasExactSynonym "HMSN1B" @default.
• MONDO_0007307 hasExactSynonym "MPZ Charcot-Marie-Tooth disease type 1" @default.
• MONDO_0007307 hasExactSynonym "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B" @default.
• MONDO_0007307 hasExactSynonym "hereditary motor and sensory neuropathy IB" @default.
• MONDO_0007307 hasRelatedSynonym "CMT 1B" @default.
• MONDO_0007307 hasRelatedSynonym "Charcot Marie Tooth disease type 1B" @default.
• MONDO_0007307 hasRelatedSynonym "Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1B" @default.
• MONDO_0007307 hasRelatedSynonym "Charcot-Marie-Tooth disease, demyelinating, type 1B" @default.
• MONDO_0007307 hasRelatedSynonym "Charcot-Marie-Tooth disease, slow nerve conduction type, linked to Duffy" @default.
• MONDO_0007307 hasRelatedSynonym "Charcot-Marie-Tooth neuropathy, type 1B" @default.
• MONDO_0007307 hasRelatedSynonym "HMSN 1B" @default.
• MONDO_0007307 hasRelatedSynonym "HMSN1" @default.
• MONDO_0007307 hasRelatedSynonym "hereditary motor and sensory neuropathy 1" @default.
• MONDO_0007307 hasRelatedSynonym "hereditary motor and sensory neuropathy 1B" @default.
• MONDO_0007307 id "MONDO:0007307" @default.
• MONDO_0007307 inSubset gard_rare @default.
• MONDO_0007307 inSubset nord_rare @default.
• MONDO_0007307 inSubset ordo_disease @default.
• MONDO_0007307 inSubset orphanet_rare @default.
• MONDO_0007307 inSubset rare @default.
• MONDO_0007307 type Class @default.
• MONDO_0007307 isDefinedBy mondo.owl @default.
• MONDO_0007307 label "Charcot-Marie-Tooth disease type 1B" @default.
• MONDO_0007307 subClassOf BFO_0000001 @default.
• MONDO_0007307 subClassOf BFO_0000002 @default.
• MONDO_0007307 subClassOf BFO_0000016 @default.
• MONDO_0007307 subClassOf BFO_0000017 @default.
• MONDO_0007307 subClassOf BFO_0000020 @default.
• MONDO_0007307 subClassOf COB_0000033 @default.
• MONDO_0007307 subClassOf COB_0000111 @default.
• MONDO_0007307 subClassOf COB_0000502 @default.
• MONDO_0007307 subClassOf MONDO_0000001 @default.
• MONDO_0007307 subClassOf MONDO_0000426 @default.
• MONDO_0007307 subClassOf MONDO_0000429 @default.
• MONDO_0007307 subClassOf MONDO_0003620 @default.
• MONDO_0007307 subClassOf MONDO_0003847 @default.
• MONDO_0007307 subClassOf MONDO_0005071 @default.
• MONDO_0007307 subClassOf MONDO_0005244 @default.
• MONDO_0007307 subClassOf MONDO_0007307 @default.
• MONDO_0007307 subClassOf MONDO_0011909 @default.
• MONDO_0007307 subClassOf MONDO_0015358 @default.
• MONDO_0007307 subClassOf MONDO_0015359 @default.
• MONDO_0007307 subClassOf MONDO_0015626 @default.
• MONDO_0007307 subClassOf MONDO_0018776 @default.
• MONDO_0007307 subClassOf MONDO_0018778 @default.
• MONDO_0007307 subClassOf MONDO_0019011 @default.
• MONDO_0007307 subClassOf MONDO_0019056 @default.
• MONDO_0007307 subClassOf MONDO_0019548 @default.
• MONDO_0007307 subClassOf MONDO_0020127 @default.
• MONDO_0007307 subClassOf MONDO_0700096 @default.
• MONDO_0007307 subClassOf OGMS_0000031 @default.
• MONDO_0007307 subClassOf PATO_0000001 @default.
• MONDO_0007307 equivalentClass B3f720cd6497d4ba5192bf5540e35ec60 @default.
• MONDO_0007307 equivalentClass Bd2a1b097f5dd57502860b179f8796b60 @default.
• MONDO_0007307 exactMatch NCIT_C118782 @default.
• MONDO_0007307 exactMatch C0270912 @default.
• MONDO_0007307 exactMatch DOID_0110152 @default.
• MONDO_0007307 exactMatch Orphanet_101082 @default.
• MONDO_0007307 exactMatch 118200 @default.
• MONDO_0007307 category Attribute @default.
• MONDO_0007307 category BiologicalEntity @default.
• MONDO_0007307 category Disease @default.
• MONDO_0007307 category DiseaseOrPhenotypicFeature @default.
• MONDO_0007307 category Entity @default.
• MONDO_0007307 category NamedThing @default.
• MONDO_0007307 category OntologyClass @default.
• MONDO_0007307 category OrganismAttribute @default.
• MONDO_0007307 category PhenotypicQuality @default.
• MONDO_0007307 category ThingWithTaxon @default.

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